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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186621Generated: October 29, 2026

Thiourea, 2-naphthalenyl- (9CI) → HCID 18537206, compound

https://huagongshe.com/reaction/2186621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiourea, 2-naphthalenyl- (9CI)HCID 2829258—
ReactantHCID 22456143HCID 22456143—
ReactantMethyl 4-(2-bromoacetyl)-5-methylthiothiophene-2-carboxylateHCID 86583828—
ProductHCID 18537206HCID 1853720680%

Reaction Steps

Methyl 5-methylthio-4-[2-(2-naphthoylamino)(1,3-thiazol-4-yl)]thiophene-2-carboxylate hydrohromide: Methyl 4-(2-bromoacetyl)-5-methylthiothiophene-2-carboxylate (65 mg, 0.21 mmol) was allowed react with 2-napthylthiourea (42.4 mg) as described in Example 154, step (a) to give 82.5 mg (80% yield) of methyl 5-methylthio-4-[2-(2-naphthylamino)(1,3-thiazol-4-yl)]thiophene-2-carboxylate hydrobromide. 1H NMR (DMSO-d6, 300 MHz) δ 2.67 (s, 3H), 3.83 (s, 3 H), 7.31 (s, 1H), 7.50-7.67 (m, 4H), 7.93 (m, 1H), 8.15 (s, 1H), 8.31-8.35 (m, 1H), 8.46 (d, 1H, J=7.6), 10.22 (s, 1H)); Mass Spectrum (ESI) m/z calcd. for C20H16N2O2S3, 412.6 (M+H), found 413.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403633B2
Source datasetuspto-grants-2002_06
ORD IDord-a89d6507035c4950acdbd27ea1c0926f
Source noteuspto-grants-2002_06