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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451747Generated: October 30, 2026

HCID 178484174, compound → HCID 178484184, compound

https://huagongshe.com/reaction/451747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178484174HCID 178484174—
SolventTrifluoroacetic acid methylene chlorideHCID 21863450—
ProductHCID 178484184HCID 17848418493%

Reaction Steps

A solution of benzyl (S)-2-(t-butoxycarbonylamino)-3-(trans-4-fluorocyclohexyl)-propyl(methyl)carbamate (200 mg, 0.47 mmol) in TFA/CH2Cl2 (15 mL, v/v 20%) was stirred for 1 h at rt, then quenched by addition of sat'd aq NaHCO3 solution until gas evolution ceased. The mixture was extracted with CH2Cl2 (2×50 mL). The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure to obtain benzyl (S)-2-amino-3-(trans-4-fluorocyclohexyl)propyl(methyl)carbamate (140 mg, yield 93%). 1HNMR (CDCl3, 400 MHz): δ 1.42 (m, 4H), 1.64 (m, 4H), 2.98 (d, 3H), 3.21 (m, 1H), 3.50 (m, 1H), 3.90 (m, 1H), 5.13 (d, 2H), 7.33 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487108B2
Source datasetuspto-grants-2013_07
ORD IDord-f2e6e3b94daf4dfe84f1892bfe4fe8d6
Source noteuspto-grants-2013_07