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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67936Generated: October 29, 2026

Water → HCID 20526351, compound

https://huagongshe.com/reaction/67936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantCID 13166207HCID 13166207—
ReactantBenzyl 3-(2-acetamidoethylthio)-7-oxo-1-azabicyclo[3.2.0]heptane-2-carboxylateHCID 14890583—
SolventChloroformHCID 6212—
ProductHCID 20526351HCID 20526351—

Reaction Steps

Benzyl 3-(2-acetamidoethylthio)-7-oxo-1-azabicyclo[3.2.0]heptane-2-carboxylate (91) (0.050 g) was dissolved in chloroform (5 ml) and stirred at 0° under argon. It was treated with water (0.010 g) and pyridine (0.022 g) followed by iodobenzene dichloride (0.038 g). A period of 2 hours was allowed to elapse and the solution was concentrated and the product chromatographed on silica gel 60 (<230 mesh) eluting with chloroform/ethanol 9:1. This gave benzyl 3-(2-acetamidoethylsulphinyl)-3-chloro-7-oxo-1-azabicyclo[3.2.0]heptane-2-carboxylate (62) (0.040 g); m.p. 89°-93°, νmax (CHCl3) 3450, 2980, 1780, 1745, 1670 and 1515 cm-1 ; τ(CDCl3) 2.70 (5H, s, phenyl), 3.70 (1H, br, NH) 4.88 (2H, s, benzyl CH2) 4.97 (1H, s, C2-H), 5.6-5.9 (1H, m, C5-H), 6.40 (2H, q J 5 Hz, NCH2), 6.6-7.0 (4H, m, SCH2 and C6-H2), 7.05 (1H, dd J 15 and 8 Hz, C4-H), 7.68 (1H, dd J 15 and 2 Hz, C4-H) and 8.07 (3H, s, COCH3); (Found; C, 52.1; H, 5.4; N, 6.9%. C18H21ClN2O5S requires C, 52.4; H, 5.1 and N, 6.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04347181
Source datasetuspto-grants-1982_08
ORD IDord-3f5e9b4cbf7148a59197094de49cfa94
Source noteuspto-grants-1982_08