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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292969Generated: October 29, 2026

Formamide → HCID 17990151, compound

https://huagongshe.com/reaction/1292969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamideHCID 713—
ReactantAmmonium formateHCID 2723923—
ReactantEthyl 2-amino-4,7-dihydro-5H-spiro[1-benzothiophere-6,2'-[1,3]dioxolane]-3-carboxylateHCID 10902110—
ProductHCID 17990151HCID 1799015188%

Reaction Conditions

Temperature140 °C

Reaction Steps

To a stirring 225 mL formamide solution of ethyl 2-amino-4,7-dihydro-5H-spiro[1-benzothiophene-6,2′-[1,3]dioxolane]-3-carboxylate (40.0 g, 0.142 mol) was added ammonium formate (17.8 g, 0.282 mol). The contents were stirred with heating at 140° C. for 16 h, after which time the heterogeneous contents were removed from heating, and allowed to cool to rt. The contents were filtered, the solid filter cake washed with water (2×60 mL), and suction dried overnight to afford the desired product as an off-white solid (33.0 g, 88%). 1H-NMR (DMSO-d6) δ 12.35 (broad s, 1H), 8.00 (s, 1H), 3.92 (s, 4H), 2.95 (t, 2H), 2.91 (s, 2H), 1.83 (t, 2H); LCMS RT=1.87 min; [M+H]+=265.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238701B2
Source datasetuspto-grants-2007_07
ORD IDord-732d866cf5fd486c8a857679e52e9c55
Source noteuspto-grants-2007_07